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Items: 1 to 20 of 142

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7094116copy number variation1nstd102humanPathogenic GRCh37 chr11: 95,523,863-95,564,420 , GRCh38.p12 chr11: 95,790,699-95,831,256 CEP57, MTMR2, 1 more genes
    nsv7060154inversion1nstd229human GRCh38 chr11: 89,626,991-96,425,689 , GRCh37.p13 chr11: 89,360,159-96,158,853 LINC02756, OSBPL9P2, 119 more genes
    nsv6907347copy number variation1nstd229human GRCh38 chr11: 89,715,432-96,566,090 , GRCh37.p13 chr11: 89,448,600-96,287,584 DISC1FP1, RPL32P25, 120 more genes
    nsv6900323copy number variation1nstd229human GRCh38 chr11: 93,200,748-96,340,159 , GRCh37.p13 chr11: 92,933,914-96,073,323 FGFR3P2, LOC112268080, 67 more genes
    nsv6637396copy number variation1nstd102humanPathogenic GRCh37 chr11: 81,478,509-104,667,040 , GRCh38.p12 chr11: 81,767,467-104,796,313 LOC107984375, RN7SL222P, 295 more genes
    nsv6634412copy number variation1nstd102humanUncertain significance GRCh37 chr11: 94,693,565-95,725,474 , GRCh38.p12 chr11: 94,960,400-95,992,310 SRSF8, LOC105369439, 25 more genes
    nsv6582429inversion1nstd223human GRCh38 chr11: 93,899,951-96,855,215 , GRCh37.p13 chr11: 93,633,117-96,726,215 MIR1260B, KDM4E, 51 more genes
    nsv6474677copy number variation1nstd223human GRCh38 chr11: 95,770,001-95,770,900 , GRCh37.p13 chr11: 95,503,165-95,504,064 FAM76B
    nsv6315537copy number variation1nstd102humanPathogenic GRCh37 chr11: 32,799,481-134,938,470 , GRCh38.p12 chr11: 32,777,935-135,068,576 PYGM, ATL3, 2125 more genes
    nsv6313961copy number variation1nstd102humanPathogenic GRCh37 chr11: 77,855,209-98,002,445 , GRCh38.p12 chr11: 78,144,163-98,131,717 MTND5P38, XIAPP2, 252 more genes
    nsv6309241copy number variation1nstd102humanUncertain significance GRCh37 chr11: 95,523,863-95,569,448 , GRCh38.p12 chr11: 95,790,699-95,836,284 MTMR2, CEP57, 1 more genes
    nsv6290834copy number variation1nstd102humanUncertain significance GRCh37 chr11: 85,422,071-118,022,671 , GRCh38.p12 chr11: 85,711,028-118,151,956 CARD17P, RNA5SP350, 480 more genes
    nsv6248358mobile element insertion1nstd215human GRCh38 chr11: 95,773,475-95,773,475 , GRCh37.p13 chr11: 95,506,639-95,506,639 FAM76B
    nsv6248357mobile element insertion1nstd215human GRCh38 chr11: 95,769,435-95,769,435 , GRCh37.p13 chr11: 95,502,599-95,502,599 FAM76B
    nsv6132294copy number variation1nstd213human GRCh37 chr11: 95,460,000-96,160,001 , GRCh38.p12 chr11: 95,726,836-96,426,837 RNA5SP345, RPL32P25, 8 more genes
    nsv5672640copy number variation1nstd102humanPathogenic GRCh37 chr11: 94,153,285-111,965,700 , GRCh38.p12 chr11: 94,420,119-112,094,976 HSPD1P13, CARD17P, 239 more genes
    nsv5380796copy number variation1nstd102humanPathogenic GRCh37 chr11: 11,835,569-118,373,112 , GRCh38.p12 chr11: 11,814,022-118,502,397 FAUP4, MMP7, 2031 more genes
    nsv5265343copy number variation1nstd204human GRCh38.p13 chr11: 95,768,801-95,780,800 , GRCh37.p13 chr11: 95,501,965-95,513,964 FAM76B
    nsv5264074copy number variation1nstd204human GRCh38.p13 chr11: 95,771,001-95,780,500 , GRCh37.p13 chr11: 95,504,165-95,513,664 FAM76B
    nsv5037979inversion1nstd200human GRCh38 chr11: 93,899,952-96,855,215 , GRCh37.p13 chr11: 93,633,118-96,726,215 , GPR83, 52 more genes
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